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RNA polymerase II primes Polycomb‐repressed developmental genes throughout terminal neuronal differentiation

Polycomb repression in mouse embryonic stem cells (ESCs) is tightly associated with promoter co‐occupancy of RNA polymerase II (RNAPII) which is thought to prime genes for activation during early development. However, it is unknown whether RNAPII poising is a general feature of Polycomb repression,...

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Autores principales: Ferrai, Carmelo, Torlai Triglia, Elena, Risner‐Janiczek, Jessica R, Rito, Tiago, Rackham, Owen JL, de Santiago, Inês, Kukalev, Alexander, Nicodemi, Mario, Akalin, Altuna, Li, Meng, Ungless, Mark A, Pombo, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658700/
https://www.ncbi.nlm.nih.gov/pubmed/29038337
http://dx.doi.org/10.15252/msb.20177754
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author Ferrai, Carmelo
Torlai Triglia, Elena
Risner‐Janiczek, Jessica R
Rito, Tiago
Rackham, Owen JL
de Santiago, Inês
Kukalev, Alexander
Nicodemi, Mario
Akalin, Altuna
Li, Meng
Ungless, Mark A
Pombo, Ana
author_facet Ferrai, Carmelo
Torlai Triglia, Elena
Risner‐Janiczek, Jessica R
Rito, Tiago
Rackham, Owen JL
de Santiago, Inês
Kukalev, Alexander
Nicodemi, Mario
Akalin, Altuna
Li, Meng
Ungless, Mark A
Pombo, Ana
author_sort Ferrai, Carmelo
collection PubMed
description Polycomb repression in mouse embryonic stem cells (ESCs) is tightly associated with promoter co‐occupancy of RNA polymerase II (RNAPII) which is thought to prime genes for activation during early development. However, it is unknown whether RNAPII poising is a general feature of Polycomb repression, or is lost during differentiation. Here, we map the genome‐wide occupancy of RNAPII and Polycomb from pluripotent ESCs to non‐dividing functional dopaminergic neurons. We find that poised RNAPII complexes are ubiquitously present at Polycomb‐repressed genes at all stages of neuronal differentiation. We observe both loss and acquisition of RNAPII and Polycomb at specific groups of genes reflecting their silencing or activation. Strikingly, RNAPII remains poised at transcription factor genes which are silenced in neurons through Polycomb repression, and have major roles in specifying other, non‐neuronal lineages. We conclude that RNAPII poising is intrinsically associated with Polycomb repression throughout differentiation. Our work suggests that the tight interplay between RNAPII poising and Polycomb repression not only instructs promoter state transitions, but also may enable promoter plasticity in differentiated cells.
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spelling pubmed-56587002017-11-01 RNA polymerase II primes Polycomb‐repressed developmental genes throughout terminal neuronal differentiation Ferrai, Carmelo Torlai Triglia, Elena Risner‐Janiczek, Jessica R Rito, Tiago Rackham, Owen JL de Santiago, Inês Kukalev, Alexander Nicodemi, Mario Akalin, Altuna Li, Meng Ungless, Mark A Pombo, Ana Mol Syst Biol Articles Polycomb repression in mouse embryonic stem cells (ESCs) is tightly associated with promoter co‐occupancy of RNA polymerase II (RNAPII) which is thought to prime genes for activation during early development. However, it is unknown whether RNAPII poising is a general feature of Polycomb repression, or is lost during differentiation. Here, we map the genome‐wide occupancy of RNAPII and Polycomb from pluripotent ESCs to non‐dividing functional dopaminergic neurons. We find that poised RNAPII complexes are ubiquitously present at Polycomb‐repressed genes at all stages of neuronal differentiation. We observe both loss and acquisition of RNAPII and Polycomb at specific groups of genes reflecting their silencing or activation. Strikingly, RNAPII remains poised at transcription factor genes which are silenced in neurons through Polycomb repression, and have major roles in specifying other, non‐neuronal lineages. We conclude that RNAPII poising is intrinsically associated with Polycomb repression throughout differentiation. Our work suggests that the tight interplay between RNAPII poising and Polycomb repression not only instructs promoter state transitions, but also may enable promoter plasticity in differentiated cells. John Wiley and Sons Inc. 2017-10-16 /pmc/articles/PMC5658700/ /pubmed/29038337 http://dx.doi.org/10.15252/msb.20177754 Text en © 2017 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Ferrai, Carmelo
Torlai Triglia, Elena
Risner‐Janiczek, Jessica R
Rito, Tiago
Rackham, Owen JL
de Santiago, Inês
Kukalev, Alexander
Nicodemi, Mario
Akalin, Altuna
Li, Meng
Ungless, Mark A
Pombo, Ana
RNA polymerase II primes Polycomb‐repressed developmental genes throughout terminal neuronal differentiation
title RNA polymerase II primes Polycomb‐repressed developmental genes throughout terminal neuronal differentiation
title_full RNA polymerase II primes Polycomb‐repressed developmental genes throughout terminal neuronal differentiation
title_fullStr RNA polymerase II primes Polycomb‐repressed developmental genes throughout terminal neuronal differentiation
title_full_unstemmed RNA polymerase II primes Polycomb‐repressed developmental genes throughout terminal neuronal differentiation
title_short RNA polymerase II primes Polycomb‐repressed developmental genes throughout terminal neuronal differentiation
title_sort rna polymerase ii primes polycomb‐repressed developmental genes throughout terminal neuronal differentiation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658700/
https://www.ncbi.nlm.nih.gov/pubmed/29038337
http://dx.doi.org/10.15252/msb.20177754
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